RESUMEN
Multiple and self-inflicted penetrating brain injuries (PBI) rare. PBI are rare. We report the case of multiple self-inflicted PBI in a 45 year old man caused by a nail gun. He was admitted to after shooting four nails into his head and one into his thorax. We review the literature on the topic and describe how this case was successfully managed in our hospital.
Asunto(s)
Craneotomía , Cuerpos Extraños/cirugía , Hueso Frontal/lesiones , Traumatismos Penetrantes de la Cabeza/etiología , Hueso Temporal/lesiones , Profilaxis Antibiótica , Lesiones Encefálicas/diagnóstico por imagen , Lesiones Encefálicas/etiología , Contraindicaciones , Urgencias Médicas , Cuerpos Extraños/diagnóstico por imagen , Cuerpos Extraños/etiología , Hueso Frontal/cirugía , Traumatismos Penetrantes de la Cabeza/diagnóstico por imagen , Humanos , Pulmón/cirugía , Lesión Pulmonar , Imagen por Resonancia Magnética , Masculino , Persona de Mediana Edad , Trastornos de la Personalidad/complicaciones , Neumotórax/etiología , Neumotórax/cirugía , Premedicación , Pronóstico , Intento de Suicidio , Hueso Temporal/cirugía , Traumatismos Torácicos/etiología , Traumatismos Torácicos/cirugía , Toracotomía , Tomografía Computarizada por Rayos XRESUMEN
Primary cerebral lymphoma (Primary CNS Lymphoma, PCNSL) is an aggressive non-Hodgkin lymphoma that originates in the central nervous system without evidence of lymphoma in any other localization at the time of diagnosis. Primary cerebral lymphomas are less well-known and are characterized than their homologues the systemic lymphomas, as they are an entity whose frequency was scarce until a few decades ago. However, the great rise in incidence that this pathology has undergone over the last three decades, and which is still unexplained, makes more studies necessary to better understand the etiopathology of this entity. Thanks to the new systems of treatment, the prognosis of this pathology has improved significantly in recent years. Nonetheless, treatment of primary cerebral lymphoma continues to give rise to numerous controversies at present due to its high neurotoxicity in patients over 60 years of age, a group of patients frequently affected by this pathology. To resolve these and other questions it is necessary to deep in the study of primary cerebral lymphoma and to carry out high quality clinical trials.
Asunto(s)
Neoplasias Encefálicas , Linfoma no Hodgkin , Neoplasias Encefálicas/complicaciones , Neoplasias Encefálicas/diagnóstico , Neoplasias Encefálicas/terapia , Femenino , Hospitales , Humanos , Linfoma Relacionado con SIDA , Linfoma no Hodgkin/complicaciones , Linfoma no Hodgkin/diagnóstico , Linfoma no Hodgkin/terapia , Masculino , Persona de Mediana Edad , EspañaRESUMEN
The bodies of the vertebrae are common locations for plasma cell diseases such as multiple myeloma and solitary plasmacytoma. Secondary invasion of the epidural space is infrequent but can cause neurological symptoms. Spinal cord compression due to pure intradural plasma cell infiltration is very rare. The authors report a 25-year-old woman who developed a progressive difficulty in walking due to a solitary spinal dural plasmacytoma. This is the first reported example in the English language literature of a purely intradural spinal plasmacytoma in a patient without other myelomatous lesions. An entirely intradural solitary plasmacytoma has a relatively better prognosis.
Asunto(s)
Plasmacitoma/diagnóstico por imagen , Plasmacitoma/patología , Neoplasias de la Médula Espinal/diagnóstico por imagen , Neoplasias de la Médula Espinal/patología , Adulto , Femenino , Humanos , Plasmacitoma/cirugía , Radiografía , Neoplasias de la Médula Espinal/cirugía , Vértebras TorácicasRESUMEN
We describe a previously diagnosed tuberous sclerosis patient that arrived to the hospital with an intracerebral hemorrhage whose origin was an arteriovenous malformation (AVM). A craniectomy was performed and the hematoma was evacuated with the alleviation of the patient. Although the association between tuberous sclerosis and intracerebral hemorrhage is known in the literature it has never been described associated with an AVM.